132 related articles for article (PubMed ID: 7673782)
1. Metabolic screening.
Thurmon TF
J La State Med Soc; 1995 Aug; 147(8):363-71. PubMed ID: 7673782
[TBL] [Abstract][Full Text] [Related]
2. Urinary screening tests in the prevention of mental deficiency.
Perry TL; Hansen S; MacDougall L
Can Med Assoc J; 1966 Jul; 95(3):89-95. PubMed ID: 5945986
[TBL] [Abstract][Full Text] [Related]
3. Inherited metabolic diseases in neurodevelopmental and neurobehavioral disorders.
Kayser MA
Semin Pediatr Neurol; 2008 Sep; 15(3):127-31. PubMed ID: 18708003
[TBL] [Abstract][Full Text] [Related]
4. [Clinical suspicion of inborn errors of metabolism].
Sperl W
Wien Klin Wochenschr; 1992; 104(16):497-502. PubMed ID: 1413807
[TBL] [Abstract][Full Text] [Related]
5. A biochemical perspective on the use of tandem mass spectrometry for newborn screening and clinical testing.
Chace DH; Kalas TA
Clin Biochem; 2005 Apr; 38(4):296-309. PubMed ID: 15766731
[TBL] [Abstract][Full Text] [Related]
6. Advances in clinical genetics. Part IV. Introduction.
Schaefer GB
Semin Pediatr Neurol; 2008 Sep; 15(3):109. PubMed ID: 18707999
[No Abstract] [Full Text] [Related]
7. Metabolic factors in the prevention of mental retardation. Compulsory screening legislation open to question.
Efron ML
R I Med J; 1967 Apr; 50(4):255-7. PubMed ID: 5232916
[No Abstract] [Full Text] [Related]
8. [Laboratory diagnosis of inborn metabolic disorders: a method for early detection of mental retardation (author's transl)].
Zimolo A
Lijec Vjesn; 1978 Jan; 100(1):75-6. PubMed ID: 642698
[No Abstract] [Full Text] [Related]
9. Newborn screening: the miracle and the challenge.
Wright L; Brown A; Davidson-Mundt A
J Pediatr Nurs; 1992 Feb; 7(1):26-42. PubMed ID: 1548559
[TBL] [Abstract][Full Text] [Related]
10. Inborn errors of metabolism in infancy and early childhood: an update.
Raghuveer TS; Garg U; Graf WD
Am Fam Physician; 2006 Jun; 73(11):1981-90. PubMed ID: 16770930
[TBL] [Abstract][Full Text] [Related]
11. [Diagnosis and acute treatment of inborn metabolic diseases in infants].
Lund AM; Christensen E; Skovby F
Ugeskr Laeger; 2002 Nov; 164(48):5613-9. PubMed ID: 12523004
[TBL] [Abstract][Full Text] [Related]
12. Prevention of mental retardation through screening, retrieval, diagnosis, and management of inherited metabolic disease.
Acosta PB
Ala J Med Sci; 1982 Oct; 19(4 Suppl 1):10-6. PubMed ID: 7149165
[No Abstract] [Full Text] [Related]
13. Metabolic evaluation of infantile epilepsy: summary recommendations of the Amalfi Group.
Buist NR; Dulac O; Bottiglieri T; Gärtner J; Rinaldo P; Wolf NI;
J Child Neurol; 2002 Dec; 17 Suppl 3():3S98-102. PubMed ID: 12597059
[TBL] [Abstract][Full Text] [Related]
14. Expanded newborn screening for genetic and metabolic disorders: modeling costs and outcomes.
Hubbard HB
Nurs Econ; 2007; 25(6):345-52. PubMed ID: 18240836
[TBL] [Abstract][Full Text] [Related]
15. [Neonatal screening for congenital metabolic disorders in Bavaria--assessment of current status and planned reorganization].
Liebl B; Roscher AA
Gesundheitswesen; 1998 Aug; 60 Suppl 1():S20-3. PubMed ID: 9816756
[TBL] [Abstract][Full Text] [Related]
16. The clinical aspects of newborn screening: importance of newborn screening follow-up.
James PM; Levy HL
Ment Retard Dev Disabil Res Rev; 2006; 12(4):246-54. PubMed ID: 17183568
[TBL] [Abstract][Full Text] [Related]
17. Human biochemical genetics: an insight into inborn errors of metabolism.
Yu C; Scott CR
J Zhejiang Univ Sci B; 2006 Feb; 7(2):165-6. PubMed ID: 16421978
[TBL] [Abstract][Full Text] [Related]
18. Perimortem laboratory investigation of genetic metabolic disorders.
Christodoulou J; Wilcken B
Semin Neonatol; 2004 Aug; 9(4):275-80. PubMed ID: 15251144
[TBL] [Abstract][Full Text] [Related]
19. Making the case for objective performance metrics in newborn screening by tandem mass spectrometry.
Rinaldo P; Zafari S; Tortorelli S; Matern D
Ment Retard Dev Disabil Res Rev; 2006; 12(4):255-61. PubMed ID: 17183573
[TBL] [Abstract][Full Text] [Related]
20. [Neonatal screening for metabolic diseases: need for efficacy studies].
Bosch AM; van Spronsen FJ
Ned Tijdschr Geneeskd; 2008 Oct; 152(43):2366-7; author reply 2367. PubMed ID: 19031509
[No Abstract] [Full Text] [Related]
[Next] [New Search]